Category: 112-59-4

Kamaura, Masahiro et al. published their research in Kidorui in 1998 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.HPLC of Formula: 112-59-4

Preparation and catalytic activity of novel water-tolerant lanthanoid alkoxide complexes was written by Kamaura, Masahiro;Daikai, Kazuhiro;Hanamoto, Takeshi;Inanaga, Junji. And the article was included in Kidorui in 1998.HPLC of Formula: 112-59-4 The following contents are mentioned in the article:

We prepared novel water-resistant lanthanoid-lithium mixed alkoxide complexes by utilizing the high coordination number of lanthanoid ions in combination with polydentate ligands. The complexes are stable and effectively catalyze the Robinson-type reaction of 2-butanone with chalcone even in the presence of water (60 equiv to the catalyst). The terbium-lithium complex of polyethylene glycol was the most effective catalyst to the above reaction. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4HPLC of Formula: 112-59-4).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.HPLC of Formula: 112-59-4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Gharagheizi, Farhad et al. published their research in Journal of Hazardous Materials in 2009 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

Prediction of upper flammability limit percent of pure compounds from their molecular structures was written by Gharagheizi, Farhad. And the article was included in Journal of Hazardous Materials in 2009.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

In this study, a quant. structure-property relationship (QSPR) is presented to predict the upper flammability limit percent (UFLP) of pure compounds The obtained model is a five parameters multi-linear equation. The parameters of the model are calculated only from chem. structure. The average absolute error and squared correlation coefficient of the obtained model over all 865 pure compounds used to develop the model are 9.7%, and 0.92, resp. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Name: 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Lim, Kyung-Hee et al. published their research in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2005 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

Temperature dependence of emulsion morphologies and the dispersion morphology diagram: Two-phase emulsions of the system C6H13(OC2H4)2OH/n-tetradecane/”water” was written by Lim, Kyung-Hee;Zhang, Wu;Smith, Gwynedd A.;Smith, Duane H.. And the article was included in Colloids and Surfaces, A: Physicochemical and Engineering Aspects in 2005.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

Using several different two-phase compositions of the pseudoternary amphiphile/oil/”water” system C6H13(OC2H4)2OH/n-tetradecane/aqueous 10 mM NaCl, it is shown by elec. conductometry that the temperature dependencies of the emulsion morphologies were consistent with predictions from the dispersion morphol. diagram, thus contradicting the phase inversion temperature (PIT) concept. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Carboxylic acid esters of low molecular weight are colourless, volatile liquids with pleasant odours, slightly soluble in water. Because of their lack of hydrogen-bond-donating ability, esters do not self-associate. Consequently, esters are more volatile than carboxylic acids of similar molecular weight.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

von Bergen, R. et al. published their research in Fluid Phase Equilibria in 1998 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

A lattice fluid approach to the concept of hydrophile lipophile balance: alkylethoxylated surfactants was written by von Bergen, R.;Rogel, E.. And the article was included in Fluid Phase Equilibria in 1998.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The relation between hydrophile lipophile balance (HLB) and the parameters of a lattice fluid equation of state (Sanchez-Lacombe) are studied. The observed linear relation between the characteristic pressure (P*) and the HLB number, probably results from the fact that both parameters are connected to the cohesive energy d. (CED). The relation between the HLB number and the number of lattice sites occupied by the alkylethoxylated surfactants in the lattice fluid model are also studied. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Quality Control of 2-(2-(Hexyloxy)ethoxy)ethanol

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Gharagheizi, Farhad et al. published their research in Industrial & Engineering Chemistry Research in 2010 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Electric Literature of C10H22O3

A New Neural Network Group Contribution Method for Estimation of Upper Flash Point of Pure Chemicals was written by Gharagheizi, Farhad;Abbasi, Reza. And the article was included in Industrial & Engineering Chemistry Research in 2010.Electric Literature of C10H22O3 The following contents are mentioned in the article:

A new group contribution-based models is presented to predict the upper flash point temperature of pure compounds based on a large dataset (1294). This neural network model uses several occurrences of 122 chem. groups in a pure compound to predict its related upper flash point limit. The model squared correlation coefficient, average percent error, mean average error, and root-mean-square error over the main dataset (1294 pure compounds) were 0.99, 1.7%, 6, and 8.5, resp. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Electric Literature of C10H22O3).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Electric Literature of C10H22O3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ranoux, Adeline et al. published their research in Science China: Chemistry in 2010 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.COA of Formula: C10H22O3

Synthesis and evaluation of C-glycosides as hydrotropes and solubilizing agents was written by Ranoux, Adeline;Lemiegre, Loic;Benvegnu, Thierry. And the article was included in Science China: Chemistry in 2010.COA of Formula: C10H22O3 The following contents are mentioned in the article:

This work presents expeditious synthesis of C-glycoside amphiphiles in aqueous media from unprotected di- or monosaccharides. A Horner-Wadsworth-Emmons/Michael addition/Barbier allylation sequence led to C-glycosides that exhibit hydrotropic properties. The hydrotropic and solubilizing properties of these homoallylic alcs. including a β-C-glycoside moiety as well as addnl. β-C-glycosidic ketones with a short (C7) alkyl chain are also described and compared with those of com. O-glucoside references This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4COA of Formula: C10H22O3).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.COA of Formula: C10H22O3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ibis, Cemil et al. published their research in Journal of Heterocyclic Chemistry in 2016 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Formula: C10H22O3

The Synthesis, Spectral, and Electrochemical Characterization of Novel Alkoxybenzoquinone Derivatives was written by Ibis, Cemil;Sahinler Ayla, Sibel;Cakan, Kadriye. And the article was included in Journal of Heterocyclic Chemistry in 2016.Formula: C10H22O3 The following contents are mentioned in the article:

The novel monosubstituted benzoquinone compounds, 2,5-O-substituted benzoquinone compounds and 2,6-O-substituted benzoquinone compounds were obtained by the reaction of p-chloranil and related alc. compounds in potassium carbonate (K2CO3) solution of acetonitrile or chloroform with Et3N. The novel cyclic compounds were obtained from the reaction of p-chloranil and diols in potassium carbonate (K2CO3) solution of acetonitrile at room temperature This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Formula: C10H22O3).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Formula: C10H22O3

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ibis, Cemil et al. published their research in Synthetic Communications in 2014 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Related Products of 112-59-4

Synthesis and Spectral and Electrochemical Characterization of Novel Substituted 1,4-Naphthoquinone Derivatives was written by Ibis, Cemil;Ayla, Sibel Sahinler;Asar, Hatice. And the article was included in Synthetic Communications in 2014.Related Products of 112-59-4 The following contents are mentioned in the article:

The novel substituted 2,3-dichloro-1,4-naphthoquinone derivatives were synthesized from the reactions of (1) and related nucleophiles in sodium carbonate (Na2CO3) solution of ethanol, chloroform with Et3N, or potassium carbonate (K2CO3) solution of acetonitrile. The structures of novel compounds were characterized by using microanal., Fourier transform-IR, 1H NMR, 13C NMR, mass spectrometry, and cyclic voltammetry (CV). This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Related Products of 112-59-4).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are also usually derived from carboxylic acids. It may also be obtained by reaction of acid anhydride or acid halides with alcohols or by the reaction of salts of carboxylic acids with alkyl halides. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Related Products of 112-59-4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Yokoyama, Shun et al. published their research in Journal of Physics and Chemistry of Solids in 2014 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol

Surface modification of Cu metal particles by the chemical reaction between the surface oxide layer and a halogen surfactant was written by Yokoyama, Shun;Takahashi, Hideyuki;Itoh, Takashi;Motomiya, Kenichi;Tohji, Kazuyuki. And the article was included in Journal of Physics and Chemistry of Solids in 2014.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

Surface oxides on small (2-5 μm) copper metal particles can be removed by chem. reaction with tris(2,3-dibromopropyl) isocyanurate (TIC) in diethylene glycol mono-n-hexyl ether (DGHE) solution under mild conditions where metal particles are not damaged. Surface oxides convert to copper bromide species and subsequently dissolve into the solvent. It was found that resultant surface species are resistant to re-oxidation due to remaining surface bromides. This finding opens up a possibility to create microclines based on cheap copper nanoparticles. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Many esters have the potential for conformational isomerism, but they tend to adopt an s-cis (or Z) conformation rather than the s-trans (or E) alternative, due to a combination of hyperconjugation and dipole minimization effects. The preference for the Z conformation is influenced by the nature of the substituents and solvent, if present. Lactones with small rings are restricted to the s-trans (i.e. E) conformation due to their cyclic structure.Application In Synthesis of 2-(2-(Hexyloxy)ethoxy)ethanol

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Grahek, R. et al. published their research in Journal of Chromatography A in 2001 | CAS: 112-59-4

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

Chromatographic purification of some 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors was written by Grahek, R.;Milivojevic, D.;Bastarda, A.;Kracun, M.. And the article was included in Journal of Chromatography A in 2001.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:

The purification of pravastatin, simvastatin and lovastatin in the sodium salt or lactone form and of mevastatin in the lactone form by reversed-phase displacement chromatog. is presented. The mobile phases consisted of water or mixtures of water-methanol and water-acetonitrile. Six different displacers were successfully used. Up to 0.14 g of raw sample per g of stationary phase was loaded on a column packed with silica-based octadecyl phase. Crude substances from 85 to 88% chromatog. purity were purified and at least 99.5% purity was achieved. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Name: 2-(2-(Hexyloxy)ethoxy)ethanol).

2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Name: 2-(2-(Hexyloxy)ethoxy)ethanol

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem